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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-08
filingDate 1994-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef580e307ee6b293f7953db86763c4db
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be4a92bab913e8b38fa87509d9e333d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b885a86aa5d3b86d012c5174210e29f
publicationDate 2001-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0707567-B1
titleOfInvention Process for the synthesis of azetidinones
abstract PCT No. PCT/US94/07291 Sec. 371 Date Jan. 4, 1996 Sec. 102(e) Date Jan. 4, 1996 PCT Filed Jul. 1, 1994 PCT Pub. No. WO95/01961 PCT Pub. Date Jan. 19, 1995This invention provides a process for preparing azetidinones useful as intermediates in the synthesis of penems and as hypocholesterolemic agents, particularly for azetidinones substituted in the C-3 and C-4 positions and optionally substituted at the ring nitrogen, comprising reacting a beta -(substituted-amino)amide, a beta -(substituted-amino)acid ester, or a beta -(substituted-amino)thiolcarbonic acid ester with a silylating agent and a cyclizing agent.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102004025071-B4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102004025071-A1
priorityDate 1993-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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